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Ahmed青光眼阀M4型(高密度多孔聚乙烯)与S2型(聚丙烯)在新生血管性青光眼患者中的安全性和有效性比较研究。

Comparative study of the safety and efficacy of the Ahmed glaucoma valve model M4 (high density porous polyethylene) and the model S2 (polypropylene) in patients with neovascular glaucoma.

作者信息

Gil-Carrasco F, Jiménez-Román J, Turati-Acosta M, Bello-López Portillo H, Isida-Llerandi C G

机构信息

Hospital Dr. Luis Sánchez Bulnes, Asociación para Evitar la Ceguera en México, Coyoacan, México.

Servicio de Glaucoma, Hospital Dr. Luis Sánchez Bulnes, Coyoacan, México.

出版信息

Arch Soc Esp Oftalmol. 2016 Sep;91(9):409-14. doi: 10.1016/j.oftal.2016.02.009. Epub 2016 Apr 8.

Abstract

OBJECTIVE

To prospectively evaluate the safety and efficacy of the Ahmed glaucoma valve model M4 (High density porous polyethylene plate; Medpor) compared with the model S2 (polypropylene plate).

METHOD

Mexican patients with neovascular glaucoma were randomly included for each group (M4 and S2). They were operated on using conventional techniques and creating a sub-episcleral tunnel to place the valve tube in the anterior chamber. After one year of follow-up, the results were evaluated with respect to a post-operative reduction in pressure, changes in visual acuity, the need for drugs, and complications, as well as the demographic characteristics of each group. Each operation using the M4 valve was performed by a single surgeon (FGC). Those operated on using the S2 model had their surgery performed by the staff surgeons at the Glaucoma Department of the Mexican Association to Prevent Blindness (APEC).

RESULTS

Each group (M4 and S2) contained 21 eyes of 21 Mexican patients with a diagnosis of neovascular glaucoma, leading to a total of 42 patients undergoing surgery. The mean preoperative intraocular pressure (IOP) was 43.5 (±11.8), and 42.24 (±12.84) mmHg for the M4 and S2 groups, respectively. After one year of follow-up, the IOP reported was 18.9 (±9.7) mmHg for the final 18 patients in the M4 group, and 16.38 (±9.76) mmHg for the 21 patients in the S2 group.

DISCUSSION

The design of a drainage valve device such as that of Ahmed has characteristics such as moderate control of IOP, thanks to the valve component in the immediate post-operative period, which makes them safer than other non-valve devices. This avoids an excess of flat chambers and the presence of low IOPs, which can lead to bleeding in the early post-operative period due to the weak desmosomal junctions of the newly formed vessels, with the advantage of maintaining suitable control of IOP from the first day after surgery.

CONCLUSION

Further studies with longer follow-up with a larger number of patients are needed to evaluate the effectiveness of this porous coating in the control of neovascular glaucoma.

摘要

目的

前瞻性评估艾哈迈德青光眼阀M4型(高密度多孔聚乙烯板;Medpor)与S2型(聚丙烯板)相比的安全性和有效性。

方法

将患有新生血管性青光眼的墨西哥患者随机纳入每组(M4和S2)。采用传统技术进行手术,并制作一个巩膜下隧道以将瓣膜管置于前房。随访一年后,评估术后眼压降低情况、视力变化、药物需求、并发症以及每组的人口统计学特征。使用M4瓣膜的每次手术均由一名外科医生(FGC)进行。使用S2型瓣膜进行手术的患者由墨西哥预防失明协会(APEC)青光眼科的外科医生进行手术。

结果

每组(M4和S2)包含21名诊断为新生血管性青光眼的墨西哥患者的21只眼,共有42名患者接受手术。M4组和S2组术前平均眼压(IOP)分别为43.5(±11.8)和42.24(±12.84)mmHg。随访一年后,M4组最后18名患者报告的眼压为18.9(±9.7)mmHg,S2组21名患者的眼压为16.38(±9.76)mmHg。

讨论

像艾哈迈德这样的引流瓣膜装置的设计具有一些特点,例如由于术后即刻的瓣膜组件,对眼压有适度控制,这使其比其他无瓣膜装置更安全。这避免了过度扁平前房和低眼压的出现,低眼压可能因新形成血管的桥粒连接薄弱而导致术后早期出血,其优点是从手术后第一天起就能维持对眼压的适当控制。

结论

需要对更多患者进行更长时间的随访研究,以评估这种多孔涂层在控制新生血管性青光眼中的有效性。

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